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AB5541

Sigma-Aldrich

Anti-Glial Fibrillary Acidic Protein Antibody

Chemicon®, from chicken

Synonym(s):

GFAP

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About This Item

UNSPSC Code:
12352203
eCl@ss:
32160702
NACRES:
NA.41

biological source

chicken

Quality Level

antibody form

affinity isolated antibody

antibody product type

primary antibodies

clone

polyclonal

purified by

affinity chromatography

species reactivity

human, mouse, rat, bovine, pig

manufacturer/tradename

Chemicon®

technique(s)

immunocytochemistry: suitable
immunohistochemistry (formalin-fixed, paraffin-embedded sections): suitable
western blot: suitable

NCBI accession no.

UniProt accession no.

shipped in

dry ice

target post-translational modification

unmodified

Gene Information

human ... GFAP(2670)

General description

Glial fibrillary acidic protein (GFAP) is a class-III intermediate filament. Type III intermediate filaments contain three domains, the most conserved of which is the rod domain. The specific sequence for this region of the protein may differ between the different intermediate filament genes for type III proteins, but the structure of the protein is highly conserved. GFAP is the main constituent of intermediate filaments in astrocytes and serves as a cell specific marker that distinguishes differentiated astrocytes from other glial cells during the development of the central nervous system. GFAP is also found in the lens epithelium, Kupffer cells of the liver, in some cells in salivary tumors and has been reported in erythrocytes.

Specificity

Expected to cross-react with bovine and porcine.
Glial fibrillary acidic protein (GFAP). Reacts with both native and recombinant protein.
Other species have not yet been tested.

Immunogen

Purified bovine GFAP.

Application

Immunohistochemistry(paraffin):
Representative images from a previous lot. Pictures of Optimal Staining With Citrate Buffer Epitope Retrieval: Human Brain.

Immunocytochemistry:
1:200-1:1,000 on cells in tissue culture fixed for one minute in 3.7% formalin and one minute in -20°C methanol.

Western blot:
1:100-1:500 using ECL. Recognizes a band of 55 kDa. May also react with a band of 50 kDa.

Immunohistochemistry:
1:100-1:500 on frozen tissue sections. Suggested fixative is 4% paraformaldehyde.

Optimal working dilutions must be determined by the end user.

STAINING PATTERN:

The antibody stains sharply defined cytoplasmic filaments of astroglia cells in tissue culture. Stains processes of astrocytes in sections of brain tissues.
This Anti-Glial Fibrillary Acidic Protein Antibody is validated for use in IC, IH, IH(P), WB for the detection of GFAP.

Quality

Routinely evaluated by Western Blot on Mouse Brain lysates.

Western Blot Analysis: 1:1000 dilution of this lot detected glial fibrillary acidic protein on 10 μg of Mouse Brain lysates.

Target description

55 kDa

Linkage

Replaces: 04-1031; 04-1062

Physical form

Purified chicken polyclonal in buffer containing PBS containing 0.02% sodium azide.

Storage and Stability

Stable for 1 year at -20°C in undiluted aliquots from date of receipt. Do not store in a self-defrosting freezer.

Handling Recommendations:
Upon first thaw, and prior to removing the cap, centrifuge the vial and gently mix the solution. Aliquot into microcentrifuge tubes and store at -20°C. Avoid repeated freeze/thaw cycles, which may damage IgG and affect product performance.

Analysis Note

Control
Astrocytes, astrocytomas, neural stem cells.

Legal Information

CHEMICON is a registered trademark of Merck KGaA, Darmstadt, Germany

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Storage Class Code

10 - Combustible liquids

WGK

WGK 2


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Tanycyte-like cells form a blood-cerebrospinal fluid barrier in the circumventricular organs of the mouse brain.
Langlet, F; Mullier, A; Bouret, SG; Prevot, V; Dehouck, B
The Journal of Comparative Neurology null
In vivo MRI analysis of an inflammatory injury in the developing brain.
Lodygensky, GA; West, T; Stump, M; Holtzman, DM; Inder, TE; Neil, JJ
Brain, behavior, and immunity null
Diffusion characteristics associated with neuronal injury and glial activation following hypoxia-ischemia in the immature brain.
Lodygensky, GA; West, T; Moravec, MD; Back, SA; Dikranian, K; Holtzman, DM; Neil, JJ
Magn. Reson. in Med. null
Increased atypical PKC expression and activity in the phrenic motor nucleus following cervical spinal injury.
Guenther, CH; Windelborn, JA; Tubon, TC; Yin, JC; Mitchell, GS
Experimental neurology null
Taurine in drinking water recovers learning and memory in the adult APP/PS1 mouse model of Alzheimer's disease.
Kim, HY; Kim, HV; Yoon, JH; Kang, BR; Cho, SM; Lee, S; Kim, JY; Kim, JW; Cho, Y; Woo, J; Kim, Y
Scientific Reports null

Articles

Explore the basics of working with antibodies including technical information on structure, classes, and normal immunoglobulin ranges.

Leverage the inherent immune ability of an animal to generate antibodies that bind to specific molecules.

Uses for immunofluorescence (IF)—where an antibody conjugated to a molecule that fluoresces when excited by lasers— include protein localization, confirmation of post-translational modification or activation, and proximity to/complexing with other proteins.

Antibodies combine with specific antigens to generate an exclusive antibody-antigen complex. Learn about the nature of this bond and its use as a molecular tag for research.

Protocols

Tips and troubleshooting for FFPE and frozen tissue immunohistochemistry (IHC) protocols using both brightfield analysis of chromogenic detection and fluorescent microscopy.

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

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